Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP501629.RALv7DlWczeqRmRSzsJ9lb_FUIYsK0xW1wv4HBSO8rFxo130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP501629.RALv7DlWczeqRmRSzsJ9lb_FUIYsK0xW1wv4HBSO8rFxo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP501629.RALv7DlWczeqRmRSzsJ9lb_FUIYsK0xW1wv4HBSO8rFxo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP501629.RALv7DlWczeqRmRSzsJ9lb_FUIYsK0xW1wv4HBSO8rFxo130_provenance.
- NP501629.RALv7DlWczeqRmRSzsJ9lb_FUIYsK0xW1wv4HBSO8rFxo130_assertion description "[Inherited biallelic mutations in the human MUTYH gene are responsible for the recessive syndrome--adenomatous colorectal polyposis (MUTYH associated polyposis, MAP)--which significantly increases the risk of colorectal cancer (CRC).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP501629.RALv7DlWczeqRmRSzsJ9lb_FUIYsK0xW1wv4HBSO8rFxo130_provenance.
- NP501629.RALv7DlWczeqRmRSzsJ9lb_FUIYsK0xW1wv4HBSO8rFxo130_assertion evidence source_evidence_literature NP501629.RALv7DlWczeqRmRSzsJ9lb_FUIYsK0xW1wv4HBSO8rFxo130_provenance.
- NP501629.RALv7DlWczeqRmRSzsJ9lb_FUIYsK0xW1wv4HBSO8rFxo130_assertion SIO_000772 15987719 NP501629.RALv7DlWczeqRmRSzsJ9lb_FUIYsK0xW1wv4HBSO8rFxo130_provenance.
- NP501629.RALv7DlWczeqRmRSzsJ9lb_FUIYsK0xW1wv4HBSO8rFxo130_assertion wasDerivedFrom befree-2016 NP501629.RALv7DlWczeqRmRSzsJ9lb_FUIYsK0xW1wv4HBSO8rFxo130_provenance.
- NP501629.RALv7DlWczeqRmRSzsJ9lb_FUIYsK0xW1wv4HBSO8rFxo130_assertion wasGeneratedBy ECO_0000203 NP501629.RALv7DlWczeqRmRSzsJ9lb_FUIYsK0xW1wv4HBSO8rFxo130_provenance.
- befree-2016 importedOn "2016-02-19" NP501629.RALv7DlWczeqRmRSzsJ9lb_FUIYsK0xW1wv4HBSO8rFxo130_provenance.